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Multi-dimensional time-correlated single photon counting (TCSPC) fluorescence lifetime imaging microscopy (FLIM) to detect FRET in cells
R. R. Duncan, A. Bergmann,
M. A. Cousin
, D. K. Apps, M. J. Shipston
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探究 'Multi-dimensional time-correlated single photon counting (TCSPC) fluorescence lifetime imaging microscopy (FLIM) to detect FRET in cells' 的科研主题。它们共同构成独一无二的指纹。
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Keyphrases
Amino Acids
16%
Cell Viability
16%
Chromophore
16%
Complex Exponential
16%
Counting Efficiency
16%
Cultured Neurons
16%
Decay Analysis
16%
Dwell Time
16%
Efficient Energy
16%
Energy Acceptor
16%
Energy Transfer Efficiency
16%
Enhanced Cyan Fluorescent Protein
33%
Enhanced Green Fluorescent Protein (eGFP)
16%
Error Range
16%
Excitation Levels
16%
Fixed-distance
16%
Fluorescence Lifetime
33%
Fluorescence Lifetime Imaging
100%
Fluorescent Lifetime
16%
Fluorescent Protein
16%
FM1-43
33%
FM4-64
16%
High Detection Efficiency
16%
High-resolution
16%
In Tandem
16%
Intrinsic Time
16%
Laser Scanning Microscope
16%
Lifetime Distribution
16%
Living Neurons
16%
Multi-exponential Decay
16%
Photobleaching
16%
Plasma Membrane
16%
Scanning Microscope
16%
Single-molecule Fluorescence Resonance Energy Transfer (smFRET)
100%
Styryl Dyes
16%
Temporal Accuracy
16%
Time-correlated Single-photon Counting (TCSPC)
100%
Transfer Condition
16%
Two Dimensional Images
16%
Engineering
Chromophore
16%
Complex Exponential
16%
Counting Efficiency
16%
Dimensional Image
16%
Dwell Time
16%
Energy Engineering
16%
Exponential Decay
16%
Fluorescence Lifetime
33%
Fluorescence Lifetime Imaging Microscopy
100%
Fluorescent Protein
66%
High Resolution
16%
Intrinsic Time
16%
Microsecond
16%
Resonance Energy
100%
Time-Correlated Single Photon Counting
100%
Two Dimensional
16%
Chemistry
Amino Acid
16%
Cell Viability
16%
Chromophore
16%
Donor
16%
Fluorescence Decay
16%
Fluorescence Lifetime
100%
Fluorescence Resonance Energy Transfer
100%
Photobleaching
16%
Chemical Engineering
Chromophore
100%